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Week of January 12–18, 2026

The week in recalls

A heavy week for medical devices, with a homecare bed and an insulin pump among the recalls. Food and vehicles filled out the list, including chicken that may carry Listeria.

Recall CanaryUpdated

Here's what got recalled this week. There were 83 recalls in all, and most were medical devices, with food and vehicles close behind. The ones that matter most are a homecare bed that can overheat and a batch of grilled chicken that may carry Listeria, so let's start there.

The chicken is Suzanna's Kitchen Grilled Chicken Breast Fillets, sold ready to eat in seven states. The product may be contaminated with Listeria, a germ that is especially hard on pregnant people, newborns, older adults and anyone with a weakened immune system. If you have these fillets in your fridge or freezer, do not eat them. Throw them away or take them back to the store, and clean anything they touched. The bed is Medline Semi Electric and Full Electric Homecare Beds. The hand control pendant and its wires can overheat, and in rare cases catch fire, particularly if the bed is pushed past its weight limit or something jams the motor. This one is rated high risk. If you use one of these beds at home, check the pendant and cord for damage and contact Medline about what to do.

Two vehicle recalls are worth a minute. Genesis G80, GV80, GV60 and GV70 Vehicles may have an instrument panel display that goes blank because of a software error, which means you could lose your speed and warning lights while driving. And Gulf Stream Trail Boss and Ameri-Lite trailers have turn signals that flash the wrong way, so other drivers may misread your intentions. The agency says do not drive these trailers until they are fixed.

That is the shape of the week. If any of these sound like something in your home or driveway, take a few minutes to check. The full list is below.

Written by Recall Canary from the agencies’ records on .

What changed

: First written on November 4 from the 83 recalls listed by then.

All 83 recalls this week

Newest first

Recalls the agencies dated Jan 12 to 18. 83 arrived after the week ended. How this list is made

23 recalls that day

Olympus ViziShot 2 FLEX (19G) EBUS -TBNA Needles

Not yet rated, FDA,

Genova Yellowfin Tuna

Not yet rated, FDA,

Suzanna's Kitchen Grilled Chicken Breast Fillets

Listeria

High risk, FSIS, , Ended

Lucid

Lucid Gravity

Backup camera defect

NHTSA,

Lucid

Lucid Air (2022-2026)

Backup camera defect

NHTSA,

Genesis

Genesis G80, GV80, GV60 and GV70 Vehicles

Electrical system defect

NHTSA,

Forest River

Forest River Freelander (2026)

Electrical system defect

NHTSA,

Winnebago

Winnebago: Spirit (2024-2026), Minnie Winnie (2024-2026), Travato (2024-2026), and 5 more

Vehicle equipment defect

NHTSA,

Lippert

Lippert Bus Windows

Driver visibility defect

NHTSA, , Part

Forest River Bus

Forest River Bus Trans Tech School Buses

Seat defect

NHTSA,

Newmar

Newmar Freedom Aire (2026)

Vehicle equipment defect

NHTSA,

Anthony's Barbecue & Dip-It Sauce

Undeclared fish

High risk, FDA, , Ended

Philips Azurion System

Software defect

Moderate risk, FDA,

RaySearch Laboratories RayStation/RayPlan Radiation Therapy Treatment Planning Systems

Device defect

Moderate risk, FDA,

ICU Medical Plum Duo and Plum Solo Infusion Pumps

Software defect

Moderate risk, FDA,

Merit Medical Inflation Devices and Custom Kits

Device defect

Moderate risk, FDA,

ICU Medical Tego Connector

Contamination

Moderate risk, FDA,

Baxter SIGMA Spectrum Infusion Pump

Device defect

Moderate risk, FDA,

Leaseir MHR Xcell Surgical Laser Instruments

Labeling error

Moderate risk, FDA,

Medline Semi Electric and Full Electric Homecare Beds

Device defect

High risk, FDA,

Mazor Robotics Mazor X Robotic Guidance System

Software defect

Moderate risk, FDA,

Southern Rocklobster Australian Greenlip Abalone

Listeria

Moderate risk, FDA, , Ended

GE Healthcare Omni Legend PET Scanners

Device defect

Moderate risk, FDA,

26 recalls that day

Live It Up Super Greens Dietary Supplement Powders

Salmonella

High risk, FDA, , Ended

Adams RealComfort and StyleWell Adirondack Patio Chairs

Fall hazard

CPSC,

Morgan Lane Asher Pajama Sets

Burn hazard

CPSC,

Greatale Self-Feeding Pillows

Suffocation hazard

CPSC,

Energizer Large Power Indicator Lanterns

Burn hazard

CPSC,

HEZI Branded Power Strips

Electric shock hazard

CPSC,

BBWOO Baby Loungers

Fall hazard

CPSC,

Frigidaire-Brand Minifridges

Fire hazard

CPSC,

Ruahouine Hair Growth Serum Bottles

Poisoning hazard

CPSC,

RootStim Beard Growth Serum

Poisoning hazard

CPSC,

R.X.Y Bicycle Helmets

Impact hazard

CPSC,

KEAWIS Crib Mattresses

Entrapment hazard

CPSC,

Ford

Ford Focus and Explorer Vehicles

Vehicle equipment defect

NHTSA,

Lincoln

Ford: Focus (2013-2018), Escape (2013-2019), and Lincoln MKC (2015-2016)

Vehicle equipment defect

NHTSA,

Ford

Ford Engine Block Heater

Vehicle equipment defect

NHTSA, , Part

Gulf Stream

Gulf Stream Trail Boss and Ameri-Lite (2026)

Do not drive

High risk, NHTSA,

Rivian

Rivian R1T (2022-2025) and R1S (2022-2026)

Seat belt defect

NHTSA,

Cipla USA Lanreotide Injection

Foreign object

Moderate risk, FDA,

ADM Animal Nutrition MasterPlex 75P 30/30 RU

Chemical contamination

High risk, FDA, , Ended

Thoratec CentriMag Blood Pump and Kits

Foreign object

Moderate risk, FDA,

Hologic ThinPrep CytoLyt Solution Buffered Cell Wash Solution

Contamination

Moderate risk, FDA,

ICU Medical Plum Duo Infusion System

Device defect

Moderate risk, FDA,

Medtronic Abre Venous Self-Expanding Stent System

Device defect

Moderate risk, FDA,

Instrumentation Laboratory Coagulation Testing Reagents

Contamination

Moderate risk, FDA,

ICU Medical Pulsator Arterial Blood Sampling Kit and Portex Spinal Tray

Device defect

Moderate risk, FDA,

Intuitive Surgical da Vinci SP Access Port Kit

Sterility problem

Moderate risk, FDA,

20 recalls that day

Encon Safety Products Aquarion Preserved Cartridges

Manufacturing problem

Moderate risk, FDA,

Advanced Pharmaceutical Technology TESTO-100 CIII Testosterone Pellets

Sterility problem

Moderate risk, FDA,

C-RAD Positioning Catalyst+ Patient Positioning Devices

Device defect

Moderate risk, FDA,

Sun Pharmaceutical Clindamycin Phosphate Topical Solution

Drug impurity

Low risk, FDA,

Philips Azurion Systems

Software defect

Moderate risk, FDA, , FDA event number 98071

PALACOS Bone Cement Mixing and Application Systems

Device defect

Moderate risk, FDA,

Healthy Truth Moringa Powder

Salmonella

High risk, FDA,

Philips Azurion Systems

Software defect

Moderate risk, FDA, , FDA event number 98096

Sanders Candy Factory Frosted Almond

Chemical contamination

Moderate risk, FDA, , Ended

Ukrop's Homestyle Foods Pound Cakes with Buttercream Icing

Undeclared soy

Moderate risk, FDA,

AZ Gems Jumbo Raw Shrimp

Chemical contamination

Moderate risk, FDA,

So Delicious Dairy Free Salted Caramel Cluster Cashewmilk Non-Dairy Frozen Dessert

Foreign object

Moderate risk, FDA, , Ended

Diagnostica Stago Asserachrom HPIA Kits

Device defect

Moderate risk, FDA,

Fran's PureBar Almondmilk Chocolate

Undeclared tree nut

High risk, FDA, , Ended

Medline Medical Procedure Convenience Kits

Device defect

Moderate risk, FDA,

Troemner Family Farm Pfeffernusse Cookies

Undeclared milk

High risk, FDA, , Ended

One Roof Atwater's Holiday Cookie Tin

Undeclared tree nut

High risk, FDA, , Ended

Alvogen Levothyroxine Sodium Tablets Thy-Tabs

Labeling error

Moderate risk, FDA,

Gold Star Distribution Advil, Aleve, Tylenol and More Over-the-Counter Medicines

Manufacturing problem

Moderate risk, FDA,

WFM Purchasing Brussel Sprouts & Kale Slaw

Undeclared egg

High risk, FDA, , Ended

7 recalls that day

East

East Trailers Beast and Beast II Trailers

Vehicle structure defect

NHTSA,

Lippert

Lippert 3000 Series Hidden Hinge Ramp Doors

Vehicle equipment defect

NHTSA, , Part

Philips Allura Xper FD10, FD20 and Biplane Systems

Device defect

Moderate risk, FDA,

Canon Medical Vantage Galan 3T and Vantage Titan 3T MRI Systems

Device defect

Moderate risk, FDA,

Elekta MOSAIQ Oncology Information System with Particle Therapy License

Foreign object

Moderate risk, FDA,

Taro Pharmaceuticals Fluocinolone Acetonide Topical Solution

Drug impurity

Low risk, FDA,

Repligen Maverick Measurement Module Spectrometer

Device defect

Moderate risk, FDA,

7 recalls that day

Outside The Breadbox Bread Crumbs

Undeclared milk

High risk, FDA, , Ended

Karison Besan Laddoo, Punjabi Pinni, Alsi Pinni and Panjiri

Undeclared milk

Moderate risk, FDA, , Ended

Spring & Mulberry Date-Sweetened Chocolate

Salmonella

High risk, FDA,

Terex

Terex: TL-Series, LT-Series, LTM40, and 3 more (2025)

Vehicle equipment defect

NHTSA,

Fresenius Kabi Ivenix Infusion System LVP Software

Software defect

Moderate risk, FDA,

HANGZHOU BEVER MEDICAL DEVICES BD Ready-to-Use Hydrophilic Catheter

Labeling error

Moderate risk, FDA,

Medline Kits With B. Braun IV Administration Sets

Device defect

Moderate risk, FDA,

How this list is made

Each recall is filed under the week of one date, a UTC calendar day. Which date depends on the agency; the recall’s own page names it.

FDA
The day FDA first posted the recall to its Enforcement Report (“Posted” on the recall page), or the day the company’s announcement appeared on FDA’s recalls page, if that came first (“Company announced”). When the day FDA posted it is not known, the day FDA classified it (“Classified”); when we listed the recall before any FDA date, the day we first listed it (“Listed on this site”). FDA’s weekly Enforcement Report, and news roundups built from it, often list the same recall a week or two later.
USDA FSIS
The day FSIS announced the recall or public health alert (“Announced”). An expanded recall keeps its first date.
CPSC
The recall date CPSC published (“Announced”).
NHTSA
The day the manufacturer filed its defect report with NHTSA (“Reported”). NHTSA publishes it days to weeks later, so vehicle recalls keep arriving after a week ends, and news coverage often comes a week or two after the week they are listed in.

Biologics are recalls by FDA’s biologics center (CBER), such as blood, tissue and vaccines, and blood bank equipment. They are usually handled by hospitals, clinics, blood banks and doctors’ offices, not bought in stores. Antibody drugs and other therapeutic biologics that FDA regulates as drugs are listed under Drugs, as FDA files them.

Once a week is over, Recall Canary writes a short post about it from the agencies’ records of that week’s listed recalls only, and rewrites it when they change. Each recall’s own page has the agency’s notice and what to check.

A recall the agency later withdrew stays listed with no risk level, and its own page is marked Withdrawn. A recall notice not yet matched to an agency record is a notice posted on the FDA or CPSC site (a company’s announcement on FDA’s site, or a CPSC news release) before it is matched to the agency’s recall record.

Not listed here: recalls by states, local agencies, other countries or other federal agencies (such as the EPA or the U.S. Coast Guard), and FDA safety alerts that are not recalls. More about dates and sources